反応式
[C:1]1([N:7]2[CH2:11][CH2:10][C:9]([NH2:12])=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:13]([O:16][C:17]1[C:22]([CH3:23])=[CH:21][C:20](N)=[CH:19][C:18]=1[CH3:25])(=[O:15])[CH3:14].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[C:13]([O:16][C:17]1[C:22]([CH3:23])=[CH:21][C:20]([NH:12][C:9]2[CH2:10][CH2:11][N:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)[N:8]=2)=[CH:19][C:18]=1[CH3:25])(=[O:15])[CH3:14]参加物
5
実験手順
4,5-Dihydro-1-phenyl-1H-pyrazol-3-amine (0.16 g), 4-amino-2,6-dimethylphenyl acetate (0.2 g), and toluene-4-sulfonic acid (0.02 g) were refluxed in toluene under nitrogen for 8 hours. Evaporation and chromatography (silica, dichloromethane/ethyl acetate [95:5]) of the residue gave the title product (0.15 g), as a solid.
後処理
- customEvaporation and chromatography (silica, dichloromethane/ethyl acetate [95:5]) of the residue
出典と根拠
- ORDレコード
- ord-6a05132bb6f6479fa1f6059fc1b38eb9
- 出典データセット
- uspto-grants-1995_06
- 特許番号
- US05428044
関連ノート
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